felt Thanks
FOR IMMEDIATE RELEASE DCM Foundation Announces Launch of Spanish Website Dublin, OH (February 7, 2024) – The DCM Foundation is thrilled to announce the launch of its website in Spanish, expanding its reach and resources to the Spanish-speaking community of Dilated Cardiomyopathy (DCM) patients and families. This landmark initiative was made possible by a generous
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It is critical that cardiomyopathy patients receive treatment from a medical center that specializes in cardiomyopathy or heart failure. It is important to note that not all cardiologists are specially trained in these two areas. When seeking expert care for your cardiomyopathy or heart failure, do not look only for a single doctor to manage your
We hope you can JOIN US for our second annual DCM Patient & Family Conference, taking place online Wednesday, October 18th from 6:00-7:30 PM ET. Click HERE to register. This year’s conference features information to help guide you on your DCM journey and three special guest speakers – all DCM patients who are living well
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The DCM Foundation Is Teaming up with the Children’s Cardiomyopathy Foundation to Call Attention to a Deadly Heart Disease The DCM Foundation is proud to partner with the Children’s Cardiomyopathy Foundation (CCF) to promote Children’s Cardiomyopathy Awareness Month throughout the month of September. The awareness month calls attention to the signs, symptoms, and risk factors for
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Please click on this link or the image above to view a recording of this webinar and learn about: Causes of DCM Symptoms of DCM and How is DCM Diagnosed Stages of Heart Failure Common Treatments for DCM Q&A Session with a Cardiologist Additional Resources & Information: Treatments for DCM: https://dcmfoundation.org/living-with-dcm/treatments-for-dcm All DCMF Recorded Webinars: https://dcmfoundation.org/webinars-news/recorded-webinars Genetics and
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Genetic Cardiomyopathy Awareness Consortium (GCAC) is Proud to Support Global Heart Hub in Their Second Annual Cardiomyopathy Awareness Week Columbus, Ohio, 26 June, 2023 – The Genetic Cardiomyopathy Awareness Consortium (“GCAC”) is excited to partner with Global Heart Hub to support the second annual Cardiomyopathy Awareness Week, taking place June 26 – July 2, 2023. This
The Global Heart Hub held a webinar earlier this spring entitled: “Why Genetics Matter.” The recording of this webinar is now available to view – please click here to watch the webinar. Additional details are below. Speakers: Prof James Ware – an expert in the field of genetics at Imperial College London Ellie Quinn –
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New initiative by Global Heart Hub aims to raise public awareness of heart disease More than 60 million people worldwide are affected by heart failure. A MAJOR global initiative during the month of May aims to raise public awareness of Heart Failure in an effort to save lives. The Global Heart Failure Awareness Month 2023
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Interested in sharing your story of genetic cardiomyopathy to help others? The DCM Foundation and the Genetic Cardiomyopathy Awareness Consortium (“GCAC”) are looking for short patient videos or written stories about genetic cardiomyopathy to share in our awareness campaign. Please submit a short video or written piece that tells your genetic cardiomyopathy story using the
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Leading up to the exciting launch of the Genetic Cardiomyopathy Awareness Consortium during our March 8th webinar, we thought it fitting to share Andrea’s story of learning that she has genetic DCM and how this has potentially saved her life… Andrea was recently diagnosed with genetic DCM at age 40, despite not having any symptoms.
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